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作 者:陈国仙[1,2] 陈建庭[1] 黄文华[3] 郑帅[1] 王国荣 林宗锦 李国山
机构地区:[1]南方医科大学南方医院脊柱骨科,广州510515 [2]福建省莆田市第一医院骨科 [3]南方医科大学临床解剖学研究所
出 处:《中国康复医学杂志》2014年第2期99-103,共5页Chinese Journal of Rehabilitation Medicine
基 金:福建省卫生厅青年基金资助项目(2011-2-49);福建莆田市科技局资助项目(2011D02)
摘 要:目的:观察不同频率振动应力对RAW264.7细胞体外诱导分化过程中,其特异性基因及骨保护素(OPG)/核因子κB受体活化因子配体(RANKL)表达的影响。方法:应用复合振动仪,将不同频段3—10Hz、15—35Hz、35—45Hz、50—70Hz和70—90Hz振动应变分别作用于体外诱导分化的RAW264.7细胞,分别为B、C、D、E、F组,未进行振动干预组为A组,振动应变加载3天和6天时,应用RT-PCR方法检测破骨细胞特异性基因(TRAP、MMP-9和CATK)与OPG/RANKL的表达水平。结果:不同振动频率组破骨细胞特异性基因表达水平逐渐减低,同时B、C、D组逐渐上调OPG基因表达,而RANKL基因的表达逐渐下调。结论:不同频率振动应力均抑制RAW264.7细胞向成熟破骨细胞增殖分化。Objective: To investigate effects of different ic genes and osteoprotegerin(OPG)/receptor cells in vitro induced differentiation process. frequency of vibration strain on the of activator for nuclear factor-r,B expression of osteoclast-specif- ligand(RANKL) in RAW264.7 Method: RAW264.7 cells were subjected to vibration strain with different frequency [3--10Hz (B-goup), 15-35Hz(C-group), 35--45Hz(D-group), 50---70Hz(E-group),70---90Hz(F-group)] and similar induced fluid. A-group cells were not subjected to vibration strain.The expressions of osteoclast-specific genes(TRAP, MMP-9 and CATK) and OPG/RANKL in osteoclasts were analyzed by semi-quantative RT-PCR. Result: In different frequency vibration groups, the expression levels of osteoclast-specific genes reduced gradu- ally, at the same time in B,C,D group vibration strain promote the expression of OPG mRNA and inhibit the expression of RANKL mRNA gradually. Conclusion: Different frequency of vibration strain can inhibit proliferation and differentiation of RAW264.7 cells into osteoclasts.
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